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Infinity External Hex Implant System

FDA UDI

Class II (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
Infinity External Hex Implant System FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
HEALING CAP Ø3.5MM .05MM HEIGHT [NOBELBIOCARE] FDA UDI
Model / Reference
54352105 FDA UDI
Description
HEALING CAP Ø3.5MM .05MM HEIGHT [NOBELBIOCARE] FDA UDI

Identifiers

Catalog Number
54352105 FDA UDI
Primary DI / UDI-DI
00614950006786 FDA UDI
510(k) Number
K954513 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 0.05 Millimeter FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Infinity External Hex Implant System by Ace Surgical Supply Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 070aaa7a-ae05-4b66-b66f-f9f88973f165 37 fields · synced May 31, 2026